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2-Amino-6-nitrobenzothiazole - >96.0%(HPLC), high purity , CAS No.6285-57-0

COA COA
    Grade & Purity:
  • ≥96%(HPLC)
In stock
Item Number
A151211
Grouped product items
SKU Size
Availability
 Price Qty
A151211-1g
1g
3
$12.90
A151211-5g
5g
3
$43.90
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Thiazoles (162)

Basic Description

Synonyms BRN 0177844 | CAS-6285-57-0 | A1221 | DTXSID3024491 | FT-0611215 | NSC-62341 | MFCD00005786 | STK353543 | Maybridge1_005516 | NCIOpen2_000006 | AC-11336 | UNII-4321510DG9 | Z104477436 | 2-Amino-6-nitrobenzothiazole, >=97% | 6-Nitro-1,3-benzothiazol-2-amin
Specifications & Purity ≥96%(HPLC)
Shipped In Normal
Product Description

Voltammetric behavior of 2-amino-6-nitrobenzothiazole has been investigated using direct current voltammetry and differential pulse voltammetry
2-Amino-6-nitrobenzothiazole has been used: . as model analyte for voltammetric determination of electrochemically reducible organic substances[4] . in the synthesis of 2-methyl-4-nitro-2H-pyrazole-3-carboxylic acid[2-(cyclohexanecarbonylamino)benzothiazol-6-yl]amide derivatives . in the preparation of push-pull nonlinear optical chromophores containing thiazole and benzothiazole acceptors . as a base in dye production by diazotation reaction

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Benzothiazoles
Subclass Not available
Intermediate Tree Nodes Not available
Direct Parent Benzothiazoles
Alternative Parents Nitroaromatic compounds  Benzenoids  2-amino-1,3-thiazoles  Heteroaromatic compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Organic zwitterions  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteropolycyclic compounds
Substituents 1,3-benzothiazole - Nitroaromatic compound - 1,3-thiazol-2-amine - Benzenoid - Azole - Thiazole - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Amine - Organic zwitterion - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as benzothiazoles. These are organic compounds containing a benzene fused to a thiazole ring (a five-membered ring with four carbon atoms, one nitrogen atom and one sulfur atom).
External Descriptors Not available

Associated Targets(Human)

DHFR Tclin Dihydrofolate reductase (3072 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Lymphoblastoid cell (5959 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HeLa (62764 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
IDO1 Tchem Indoleamine 2,3-dioxygenase (6650 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Leishmania infantum (5912 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Trichomonas vaginalis (2376 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Giardia intestinalis (1290 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Vero (26788 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PTR1 Pteridine reductase 1 (345 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504753095
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504753095
IUPAC Name 6-nitro-1,3-benzothiazol-2-amine
INCHI InChI=1S/C7H5N3O2S/c8-7-9-5-2-1-4(10(11)12)3-6(5)13-7/h1-3H,(H2,8,9)
InChIKey GPNAVOJCQIEKQF-UHFFFAOYSA-N
Smiles C1=CC2=C(C=C1[N+](=O)[O-])SC(=N2)N
Isomeric SMILES C1=CC2=C(C=C1[N+](=O)[O-])SC(=N2)N
WGK Germany 2
RTECS DL0865000
UN Number 2811
Packing Group I
Molecular Weight 195.2
Beilstein 27(2)232
Reaxy-Rn 177844
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=177844&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot Number Certificate Type Date Item
B2428311 Certificate of Analysis Jan 25, 2024 A151211
B2428308 Certificate of Analysis Jan 25, 2024 A151211
B2428309 Certificate of Analysis Jan 25, 2024 A151211
B2428310 Certificate of Analysis Jan 25, 2024 A151211

Chemical and Physical Properties

Melt Point(°C) 247 - 249 °C
Molecular Weight 195.200 g/mol
XLogP3 2.100
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 5
Rotatable Bond Count 0
Exact Mass 195.01 Da
Monoisotopic Mass 195.01 Da
Topological Polar Surface Area 113.000 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 220.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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